Cristiano Fava
Department of Clinical Sciences
Lund University
University Hospital of Malmö
Sweden
Name/email consistency: high
- Prediction of blood pressure changes over time and incidence of hypertension by a genetic risk score in Swedes. Fava, C., Sjögren, M., Montagnana, M., Danese, E., Almgren, P., Engström, G., Nilsson, P., Hedblad, B., Guidi, G.C., Minuz, P., Melander, O. Hypertension (2013)
- The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmö Diet and cancer study. Fava, C., Montagnana, M., Danese, E., Sjögren, M., Almgren, P., Engström, G., Hedblad, B., Guidi, G.C., Minuz, P., Melander, O. BMC Med. Genet. (2012)
- Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes. Fava, C., Danese, E., Montagnana, M., Sjögren, M., Almgren, P., Engström, G., Nilsson, P., Hedblad, B., Guidi, G.C., Minuz, P., Melander, O. J. Hypertens. (2011)
- The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes. Fava, C., Montagnana, M., Almgren, P., Hedblad, B., Engström, G., Berglund, G., Minuz, P., Melander, O. J. Hypertens. (2010)
- Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes. Fava, C., Montagnana, M., Danese, E., Almgren, P., Hedblad, B., Engström, G., Berglund, G., Minuz, P., Melander, O. Pharmacogenet. Genomics (2010)
- Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome. Fava, C., Montagnana, M., Guerriero, M., Almgren, P., von Wowern, F., Minuz, P., Melander, O. J. Hypertens. (2009)
- The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure. Fava, C., Montagnana, M., Almgren, P., Rosberg, L., Lippi, G., Hedblad, B., Engström, G., Berglund, G., Minuz, P., Melander, O. Hypertension (2008)
- Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure. Fava, C., Montagnana, M., Rosberg, L., Burri, P., Almgren, P., Jönsson, A., Wanby, P., Lippi, G., Minuz, P., Hulthèn, L.U., Aurell, M., Melander, O. Hum. Mol. Genet. (2008)
- Determinants of kidney function in Swedish families: role of heritable factors. Fava, C., Montagnana, M., Burri, P., Almgren, P., Minuz, P., Hulthén, U.L., Melander, O. J. Hypertens. (2008)
- Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender. Fava, C., Montagnana, M., Almgren, P., Rosberg, L., Guidi, G.C., Berglund, G., Melander, O. Am. J. Hypertens. (2007)
- The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes. Fava, C., Montagnana, M., Almgren, P., Rosberg, L., Guidi, G.C., Berglund, G., Melander, O. J. Hypertens. (2007)
- Determinants of diastolic dysfunction: a geometric matter?. Fava, C. Am. J. Hypertens. (2007)
- In the name of the father... and the mother. Fava, C. Am. J. Hypertens. (2006)
